Trials / Unknown
UnknownNCT03609736
PSMA-based 18F-DCFPyL PET/CT: Evaluating Its Application in Real Life
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 12 (estimated)
- Sponsor
- Grand River Hospital · Academic / Other
- Sex
- Male
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to provide pilot data on the clinical situations in which ordering a 18F-DCFPyL positron emission tomography/computed tomography (PET/CT) was thought to be clinically useful, and to document how the results of the 18F-DCFPyL PET/CT affected patient management. The results of this study could then serve as a guide to help OHIP to consider these scenarios when deciding the precise indications for funded 18F-DCFPyL PET/CT scans in the future. In this study the investigators will image subjects with prostate cancer using 18F-DCFPyL PET/CT and record how the result of the study affected patient management.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | 18F-DCFPyL PET/CT | * A bolus of less than or equal to 9 mCi (333 MBq) of 18F-DCFPyL will be injected IV by slow IV push. * After administration of the 18F-DCFPyL the line will be flushed with saline (0.9% w/v). * Subjects should be encouraged to drink up to 500 mL of water shortly after the administration of 18F-DCFPyL. * At 60-minutes (± 10 minutes) after administration of 18F-DCFPyL, the PET/CT scan will be acquired with the subject in the supine position and the FOV including the mid-thighs to skull base. |
Timeline
- Start date
- 2018-08-10
- Primary completion
- 2019-08-01
- Completion
- 2019-12-01
- First posted
- 2018-08-01
- Last updated
- 2019-02-15
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT03609736. Inclusion in this directory is not an endorsement.